Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
59001 BAA01g31600 A01 20672888 G A upstream_gene_variant MODIFIER c.-1156C>T| S65
59002 BAA01g31600 A01 20673413 G A upstream_gene_variant MODIFIER c.-1681C>T| S65
59003 BAA01g31600 A01 20673621 G A upstream_gene_variant MODIFIER c.-1889C>T| S302
59004 BAA01g31610 A01 20673889 C T missense_variant MODERATE c.2137G>A|p.Asp713Asn S131
59005 BAA01g31610 A01 20674207 C T missense_variant MODERATE c.1819G>A|p.Asp607Asn S179
59006 BAA01g31610 A01 20674285 C T missense_variant MODERATE c.1741G>A|p.Asp581Asn S161
59007 BAA01g31610 A01 20674877 G A missense_variant MODERATE c.1208C>T|p.Ser403Leu S38
59008 BAA01g31610 A01 20675115 G A missense_variant MODERATE c.970C>T|p.Pro324Ser S87
59009 BAA01g31610 A01 20675128 G A synonymous_variant LOW c.957C>T|p.Arg319Arg S229
59010 BAA01g31610 A01 20675352 C T missense_variant MODERATE c.733G>A|p.Val245Ile S81
S85
59011 BAA01g31600 A01 20676147 C T upstream_gene_variant MODIFIER c.-4415G>A| S235
59012 BAA01g31610 A01 20677808 T G upstream_gene_variant MODIFIER c.-1724A>C| S286
59013 BAA01g31610 A01 20677877 G A upstream_gene_variant MODIFIER c.-1793C>T| S87
59014 BAA01g31610 A01 20678044 C T upstream_gene_variant MODIFIER c.-1960G>A| S303
59015 BAA01g31610 A01 20678781 G A upstream_gene_variant MODIFIER c.-2697C>T| S274
59016 BAA01g31610 A01 20678883 C T upstream_gene_variant MODIFIER c.-2799G>A| S94
59017 BAA01g31610 A01 20679256 C T upstream_gene_variant MODIFIER c.-3172G>A| S48
59018 BAA01g31610 A01 20679603 G A upstream_gene_variant MODIFIER c.-3519C>T| S84
S93
59019 BAA01g31610 A01 20679730 C T upstream_gene_variant MODIFIER c.-3646G>A| S66
59020 BAA01g31620 A01 20680437 G A missense_variant MODERATE c.1190C>T|p.Pro397Leu S149
59021 BAA01g31620 A01 20681361 C T missense_variant MODERATE c.613G>A|p.Ala205Thr S165
59022 BAA01g31620 A01 20681599 G A synonymous_variant LOW c.375C>T|p.Thr125Thr S241
59023 BAA01g31620 A01 20681781 C T splice_acceptor_variant&intron_variant HIGH c.194-1G>A| S168
59024 BAA01g31620 A01 20681984 C T missense_variant MODERATE c.79G>A|p.Glu27Lys S203
59025 BAA01g31620 A01 20681992 C T missense_variant&splice_region_variant MODERATE c.71G>A|p.Cys24Tyr S88